Genomic surveillance of SARS-CoV-2 during the first year of the pandemic in the Bronx enabled clinical and epidemiological inference.
J Maximilian FelsSaad KhanRyan ForsterKarin A SkalinaSurksha SirichandAmy S FoxAviv BergmanWilliam B MitchellLucia R WolgastWendy A SzymczakRobert H BortzM Eugenia DieterleCatalina FlorezDenise HaslwanterRohit K JangraEthan LaudermilchAriel S WirchnianskiJason BarnhillDavid L GoldmanHnin KhineD Yitzchak GoldsteinJohanna P DailyKartik ChandranLibusha KellyPublished in: Cold Spring Harbor molecular case studies (2022)
The Bronx was an early epicenter of the COVID-19 pandemic in the USA. We conducted temporal genomic surveillance of 104 SARS-CoV-2 genomes across the Bronx from March October 2020. Although the local structure of SARS-CoV-2 lineages mirrored those of New York City and New York State, temporal sampling revealed a dynamic and changing landscape of SARS-CoV-2 genomic diversity. Mapping the trajectories of mutations, we found that while some became 'endemic' to the Bronx, other, novel mutations rose in prevalence in the late summer/early fall. Geographically resolved genomes enabled us to distinguish between cases of reinfection and persistent infection in two pediatric patients. We propose that limited, targeted, temporal genomic surveillance has clinical and epidemiological utility in managing the ongoing COVID pandemic.